Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 6
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 3
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 2
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 2
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 1
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 1
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 1
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 1
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 1
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 1
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 2
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 3
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 4
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5